Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities. - Wikidata - awgldk - TriplyDB

Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities.

Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities.

http://www.wikidata.org/entity/Q35011856

about

Reduced transcription of TCOF1 in adult cells of Treacher Collins syndrome patients The "domestication syndrome" in mammals: a unified explanation based on neural crest cell behavior and genetics Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate Treacher Collins syndrome: etiology, pathogenesis and prevention Haploinsufficiency of a spliceosomal GTPase encoded by EFTUD2 causes mandibulofacial dysostosis with microcephaly Treacher Collins syndrome: unmasking the role of Tcof1/treacle Applications of Mesenchymal Stem Cells and Neural Crest Cells in Craniofacial Skeletal Research Ribosomopathies: Global process, tissue specific defects Ribosomopathies: how a common root can cause a tree of pathologies Facial dysostoses: Etiology, pathogenesis and management Guarding the 'translation apparatus': defective ribosome biogenesis and the p53 signaling pathway Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome Diverse diseases from a ubiquitous process: the ribosomopathy paradox Irf6 is a key determinant of the keratinocyte proliferation-differentiation switch PI3K-mediated PDGFRα signaling regulates survival and proliferation in skeletal development through p53-dependent intracellular pathways CRISPR/Cas9 allows efficient and complete knock-in of a destabilization domain-tagged essential protein in a human cell line, allowing rapid knockdown of protein function Elongation factor 1 alpha1 and genes associated with Usher syndromes are downstream targets of GBX2 Altered mRNA Splicing, Chondrocyte Gene Expression and Abnormal Skeletal Development due to SF3B4 Mutations in Rodriguez Acrofacial Dysostosis Regulatory variant in FZD6 gene contributes to nonsyndromic cleft lip and palate in an African-American family Insights into neural crest development and evolution from genomic analysis Bmp2 is required for cephalic neural tube closure in the mouse Cell-fate determination by ubiquitin-dependent regulation of translation A neuroprotective phase precedes striatal degeneration upon nucleolar stress.The old and new face of craniofacial research: How animal models inform human craniofacial genetic and clinical data Folate deficiency facilitates recruitment of upstream binding factor to hot spots of DNA double-strand breaks of rRNA genes and promotes its transcription A p53-dependent mechanism underlies macrocytic anemia in a mouse model of human 5q- syndrome.Ribosome biogenesis in skeletal development and the pathogenesis of skeletal disorders The dichotomy of p53 regulation by noncoding RNAs.Cleft lip and palate genetics and application in early embryological development.Ribosomopathies: human disorders of ribosome dysfunction.Functional analysis of the zebrafish ortholog of HMGCS1 reveals independent functions for cholesterol and isoprenoids in craniofacial development.Regulation of BLM Nucleolar Localization Fishing the molecular bases of Treacher Collins syndrome Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome.Ribosome defects in disorders of erythropoiesis.Nucleolar stress with and without p53.Mammalian neurogenesis requires Treacle-Plk1 for precise control of spindle orientation, mitotic progression, and maintenance of neural progenitor cells.When ribosomes go bad: diseases of ribosome biogenesis.Cockayne syndrome protein A is a transcription factor of RNA polymerase I and stimulates ribosomal biogenesis and growth Ribosomopathies: mechanisms of disease.

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P2860

Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities.

http://www.wikidata.org/entity/Q35011856

description

2006 nî lūn-bûn

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2006 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի օգոստոսին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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Tcof1/Treacle is required for ...... se craniofacial abnormalities.

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PNAS.0603730103

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Proceedings of the National Academy of Sciences of the United States of America

P1476

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P2093

Jean-Philippe Rey

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Jennifer Crane

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Jill Dixon

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Lisa L Sandell

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Michael J Dixon

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Natalie C Jones

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Paul A Trainor

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Sachintha M Jayasinghe

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P2860

Compound developmental eye disorders following inactivation of TGFbeta signaling in neural-crest stem cells.

Neural Crest and the Origin of Vertebrates: A New Head

The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor

TOR regulates ribosomal protein gene expression via PKA and the Forkhead transcription factor FHL1.

The Treacher Collins syndrome (TCOF1) gene product is involved in pre-rRNA methylation

Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome. The Treacher Collins Syndrome Collaborative Group

Mutations in the Treacher Collins syndrome gene lead to mislocalization of the nucleolar protein treacle

The transcription factor snail controls epithelial-mesenchymal transitions by repressing E-cadherin expression

Monoclonal antibodies to nucleic acid-containing cellular constituents: probes for molecular biology and autoimmune disease

Canonical Wnt activity regulates trunk neural crest delamination linking BMP/noggin signaling with G1/S transition.

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13403-13408

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10.1073/PNAS.0603730103

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36

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103

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2006-08-28T00:00:00Z

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6849619

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16938878

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1557391

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